EGFR c.2702-1056A>T

Variant ID: 7-55265354-A-T

NM_005228.3(EGFR):c.2702-1056A>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs2740763
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Association of Polymorphisms in Connective Tissue Growth Factor and Epidermal Growth Factor Receptor Genes With Human Longevity.

The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences
Donlon, Timothy A TA; Morris, Brian J BJ; He, Qimei Q; Chen, Randi R; Masaki, Kamal H KH; Allsopp, Richard C RC; Willcox, D Craig DC; Tranah, Gregory J GJ; Parimi, Neeta N; Evans, Daniel S DS; Flachsbart, Friederike F; Nebel, Almut A; Kim, Duk-Hwan DH; Park, Joobae J; Willcox, Bradley J BJ
Publication Date: 2017-08-01

Variant appearance in text: rs2740763
PubMed Link: 27365368
Variant Present in the following documents:
  • Main text
View BVdb publication page



A two-stage case-control study of EGFR polymorphisms and breast cancer risk.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Hong, Young-Seoub YS; Deming, Sandra L SL; Gao, Yu-Tang YT; Long, Ji-Rong JR; Shu, Xiao-Ou XO; Cai, Qiuyin Q; Lu, Wei W; Zheng, Wei W
Publication Date: 2009-02

Variant appearance in text: rs2740763
PubMed Link: 19190167
Variant Present in the following documents:
  • Main text
View BVdb publication page